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Ansgar Schulz

Showing results (31-40 of 134) with videos related to

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Frontiers in Immunology|August 30, 2018
Joint Modeling of Immune Reconstitution Post Haploidentical Stem Cell Transplantation in Pediatric Patients With Acute Leukemia Comparing CD34<sup>+</sup>-Selected to CD3/CD19-Depleted Grafts in a Retrospective Multicenter StudyEmilia Salzmann-Manrique, Melanie Bremm, Sabine Huenecke, et al.
Haematologica|October 29, 2013
Treosulfan-based conditioning regimen for children and adolescents with hemophagocytic lymphohistiocytosisKai Lehmberg, Michael H Albert, Rita Beier, et al.
Clinical Immunology (Orlando, Fla.)|January 7, 2024
Chemotherapy for a secondary malignancy nearly restores complete chimerism in an SCID-patient after HSCTFelix I Maier, Ansgar Schulz, Ingrid Furlan, et al.
Ticks and Tick-Borne Diseases|November 24, 2019
Epidemiological investigations of Crimean-Congo haemorrhagic fever virus infection in sheep and goats in Balochistan, PakistanKhushal Khan Kasi, Miriam Andrada Sas, Carola Sauter-Louis, et al.
Cancer Immunology, Immunotherapy : CII|March 21, 2002
Ocular symptoms in children treated with human-mouse chimeric anti-GD2 mAb ch14.18 for neuroblastomaBernhard Kremens, Barbara Hero, Joachim Esser, et al.
The Journal of Pediatrics|May 19, 2015
Unmistakable Morphology? Infantile Malignant Osteopetrosis Resembling Juvenile Myelomonocytic Leukemia in InfantsAnne Strauss, Ingrid Furlan, Sandra Steinmann, et al.
Nature Genetics|December 2, 2008
Reticular dysgenesis (aleukocytosis) is caused by mutations in the gene encoding mitochondrial adenylate kinase 2Ulrich Pannicke, Manfred Hönig, Isabell Hess, et al.
European Journal of Haematology|September 13, 2023
Long-term haematological response and maintained immunological function after laparoscopic subtotal splenectomy in patients with hereditary spherocytosisAlica L Münch, Eva-Maria Jacobsen, Ansgar Schulz, et al.
Data in Brief|September 14, 2019
Dataset of clinical, immunohistopathological and laboratory features of patients with MHC II deficiency suffering from enteropathyCarsten Posovszky, Mehtap Sirin, Eva Jacobsen, et al.
European Journal of Human Genetics : EJHG|June 15, 2017
Coexisting variants in OSTM1 and MANEAL cause a complex neurodegenerative disorder with NBIA-like brain abnormalitiesDiran Herebian, Bader Alhaddad, Annette Seibt, et al.
Pageof 14

Showing results (31-40 of 134) with videos related to

Sort By:
Pageof 14
Frontiers in Immunology|August 30, 2018
Joint Modeling of Immune Reconstitution Post Haploidentical Stem Cell Transplantation in Pediatric Patients With Acute Leukemia Comparing CD34<sup>+</sup>-Selected to CD3/CD19-Depleted Grafts in a Retrospective Multicenter StudyEmilia Salzmann-Manrique, Melanie Bremm, Sabine Huenecke, et al.
Haematologica|October 29, 2013
Treosulfan-based conditioning regimen for children and adolescents with hemophagocytic lymphohistiocytosisKai Lehmberg, Michael H Albert, Rita Beier, et al.
Clinical Immunology (Orlando, Fla.)|January 7, 2024
Chemotherapy for a secondary malignancy nearly restores complete chimerism in an SCID-patient after HSCTFelix I Maier, Ansgar Schulz, Ingrid Furlan, et al.
Ticks and Tick-Borne Diseases|November 24, 2019
Epidemiological investigations of Crimean-Congo haemorrhagic fever virus infection in sheep and goats in Balochistan, PakistanKhushal Khan Kasi, Miriam Andrada Sas, Carola Sauter-Louis, et al.
Cancer Immunology, Immunotherapy : CII|March 21, 2002
Ocular symptoms in children treated with human-mouse chimeric anti-GD2 mAb ch14.18 for neuroblastomaBernhard Kremens, Barbara Hero, Joachim Esser, et al.
The Journal of Pediatrics|May 19, 2015
Unmistakable Morphology? Infantile Malignant Osteopetrosis Resembling Juvenile Myelomonocytic Leukemia in InfantsAnne Strauss, Ingrid Furlan, Sandra Steinmann, et al.
Nature Genetics|December 2, 2008
Reticular dysgenesis (aleukocytosis) is caused by mutations in the gene encoding mitochondrial adenylate kinase 2Ulrich Pannicke, Manfred Hönig, Isabell Hess, et al.
European Journal of Haematology|September 13, 2023
Long-term haematological response and maintained immunological function after laparoscopic subtotal splenectomy in patients with hereditary spherocytosisAlica L Münch, Eva-Maria Jacobsen, Ansgar Schulz, et al.
Data in Brief|September 14, 2019
Dataset of clinical, immunohistopathological and laboratory features of patients with MHC II deficiency suffering from enteropathyCarsten Posovszky, Mehtap Sirin, Eva Jacobsen, et al.
European Journal of Human Genetics : EJHG|June 15, 2017
Coexisting variants in OSTM1 and MANEAL cause a complex neurodegenerative disorder with NBIA-like brain abnormalitiesDiran Herebian, Bader Alhaddad, Annette Seibt, et al.
Pageof 14